New 1,4-naphthalenedicarboxylic acid- and 3,5-bis(benzimidazol-2-yl)pyridine-appended d10-configuration-based coordination polymers as recoverable turn-off luminescent sensors for tetracycline

被引:0
|
作者
Xiao, Yao [1 ]
Luo, Jing [1 ]
Wang, Jun [1 ]
Lu, Lu [1 ]
Prakash, Om [2 ]
Srivastava, Shreya [2 ]
Muddassir, Mohd. [3 ]
Kumar, Abhinav [2 ]
机构
[1] Sichuan Univ Sci & Engn, Sch Chem & Environm Engn, Zigong 643000, Peoples R China
[2] Univ Lucknow, Fac Sci, Dept Chem, Lucknow 226007, India
[3] King Saud Univ, Coll Sci, Dept Chem, Riyadh 11451, Saudi Arabia
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; INTERMOLECULAR INTERACTIONS; HIRSHFELD SURFACES; FLUORESCENT SENSOR;
D O I
10.1039/d5dt00025d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Coordination polymers (CPs) possessing Zn2+ and Cd2+ display interesting photoluminescent properties, thereby finding utility as luminescent sensors to detect traces of molecular substances. Herein, new Cd(ii) and Zn(ii)-based coordination polymers (CPs) with formulae [Cd3(L)3(3,5-bipy)6(H2O)3<middle dot>H2L<middle dot>5H2O] (1) and [Zn(HL)2(3,5-bipy)2] (2) were synthesized utilizing 1,4-naphthalenedicarboxylic acid (H2L) as the main ligand and 3,5-bis(benzimidazol-2-yl)pyridine (3,5-bipy) as the co-ligand and characterized. These CPs exhibited luminescent properties. Upon exciting their aqueous suspensions at 360 nm, both 1 and 2 exhibited broad emissions at 461 nm and 457 nm, respectively, with 1 displaying more intense emission than 2. Furthermore, employing these CPs as luminescent sensors for sensing antibiotics in aqueous media suggest that both 1 and 2 display selective and sensitive sensing towards tetracycline (TCY). 1 and 2 demonstrated limit of detection (LOD) values of 6.21 x 10-6 M and 1.07 x 10-5 M, respectively, accompanied with Stern-Volmer constants (Ksv) of 2.08 x 104 M-1 and 1.24 x 104 M-1. Additionally, recoveries in the luminescent responses of both 1 and 2 were successfully achieved through titration-back experiments using salicylic acid (SA). The integrated experimental and computational techniques suggest that the decline in emission intensity of CPs in the presence of antibiotics is due to energy/charge transfer and interaction with TCY, inducing minor alterations in the framework. These alterations form a non-fluorescent ground state complex (GSC) that alters the electron communication and decreases the photoluminescent intensity. Also, restoration in the emissive responses of TCY@CP arises due to the SA-assisted release of TCY from TCY@CP, which leads to restoration of the emissive responses.
引用
收藏
页码:5888 / 5895
页数:8
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